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295 related items for PubMed ID: 12928481
1. The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants. van Heel DA, Dechairo BM, Dawson G, McGovern DP, Negoro K, Carey AH, Cardon LR, Mackay I, Jewell DP, Lench NJ. Hum Mol Genet; 2003 Oct 15; 12(20):2569-75. PubMed ID: 12928481 [Abstract] [Full Text] [Related]
2. Contribution of OCTN variants within the IBD5 locus to pediatric onset Crohn's disease. Babusukumar U, Wang T, McGuire E, Broeckel U, Kugathasan S. Am J Gastroenterol; 2006 Jun 15; 101(6):1354-61. PubMed ID: 16771961 [Abstract] [Full Text] [Related]
3. The contribution of OCTN1/2 variants within the IBD5 locus to disease susceptibility and severity in Crohn's disease. Noble CL, Nimmo ER, Drummond H, Ho GT, Tenesa A, Smith L, Anderson N, Arnott ID, Satsangi J. Gastroenterology; 2005 Dec 15; 129(6):1854-64. PubMed ID: 16344054 [Abstract] [Full Text] [Related]
4. Evidence for association of OCTN genes and IBD5 with ulcerative colitis. Waller S, Tremelling M, Bredin F, Godfrey L, Howson J, Parkes M. Gut; 2006 Jun 15; 55(6):809-14. PubMed ID: 16361305 [Abstract] [Full Text] [Related]
6. Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers. Crawford NP, Colliver DW, Funke AA, Young MN, Kelley S, Cobbs GA, Petras RE, Galandiuk S. Hum Mutat; 2005 Feb 15; 25(2):156-66. PubMed ID: 15643611 [Abstract] [Full Text] [Related]
7. Clinical applications of NOD2/CARD15 mutations in Crohn's disease. Barreiro-de Acosta M, Peña AS. Acta Gastroenterol Latinoam; 2007 Mar 15; 37(1):49-54. PubMed ID: 17486745 [Abstract] [Full Text] [Related]
8. Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population. Ernst A, Jacobsen B, Østergaard M, Okkels H, Andersen V, Dagiliene E, Pedersen IS, Thorsgaard N, Drewes AM, Krarup HB. Scand J Gastroenterol; 2007 Dec 15; 42(12):1445-51. PubMed ID: 17852840 [Abstract] [Full Text] [Related]
9. [NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study]. Lakatos L, Lakatos PL, Willheim-Polli C, Reinisch W, Ferenci P, Tulassay Z, Molnár T, Kovács A, Papp J, Szalay F, Hungarian IBD Study Group. Orv Hetil; 2004 Jul 04; 145(27):1403-11. PubMed ID: 15320482 [Abstract] [Full Text] [Related]
10. No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease. de Jong DJ, Franke B, Naber AH, Willemen JJ, Heister AJ, Brunner HG, de Kovel CG, Hol FA. Eur J Hum Genet; 2003 Nov 04; 11(11):884-7. PubMed ID: 14571275 [Abstract] [Full Text] [Related]
11. Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population. Bianchi V, Maconi G, Ardizzone S, Colombo E, Ferrara E, Russo A, Tenchini ML, Porro GB. Eur J Gastroenterol Hepatol; 2007 Mar 04; 19(3):217-23. PubMed ID: 17301648 [Abstract] [Full Text] [Related]
12. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies. van der Linde K, Boor PP, Houwing-Duistermaat JJ, Crusius BJ, Wilson PJ, Kuipers EJ, de Rooij FW. Eur J Gastroenterol Hepatol; 2007 Jun 04; 19(6):449-59. PubMed ID: 17489054 [Abstract] [Full Text] [Related]
13. Association of organic cation transporter risk haplotype with perianal penetrating Crohn's disease but not with susceptibility to IBD. Vermeire S, Pierik M, Hlavaty T, Claessens G, van Schuerbeeck N, Joossens S, Ferrante M, Henckaerts L, Bueno de Mesquita M, Vlietinck R, Rutgeerts P. Gastroenterology; 2005 Dec 04; 129(6):1845-53. PubMed ID: 16344053 [Abstract] [Full Text] [Related]
14. Lack of association between IBD5 and Crohn's disease in Japanese patients demonstrates population-specific differences in inflammatory bowel disease. Tosa M, Negoro K, Kinouchi Y, Abe H, Nomura E, Takagi S, Aihara H, Oomori S, Sugimura M, Takahashi K, Hiwatashi N, Takahashi S, Shimosegawa T. Scand J Gastroenterol; 2006 Jan 04; 41(1):48-53. PubMed ID: 16373276 [Abstract] [Full Text] [Related]
15. Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease genetics. van Heel DA, McGovern DP, Cardon LR, Dechairo BM, Lench NJ, Carey AH, Jewell DP. Am J Med Genet; 2002 Aug 15; 111(3):253-9. PubMed ID: 12210321 [Abstract] [Full Text] [Related]
16. Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility loci. Paavola-Sakki P, Ollikainen V, Heliö T, Halme L, Turunen U, Lahermo P, Lappalainen M, Färkkilä M, Kontula K. Eur J Hum Genet; 2003 Feb 15; 11(2):112-20. PubMed ID: 12634858 [Abstract] [Full Text] [Related]
17. Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease. Negoro K, McGovern DP, Kinouchi Y, Takahashi S, Lench NJ, Shimosegawa T, Carey A, Cardon LR, Jewell DP, van Heel DA. Gut; 2003 Apr 15; 52(4):541-6. PubMed ID: 12631666 [Abstract] [Full Text] [Related]
18. CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins. Halfvarson J, Bresso F, D'Amato M, Järnerot G, Pettersson S, Tysk C. Dig Liver Dis; 2005 Oct 15; 37(10):768-72. PubMed ID: 16002353 [Abstract] [Full Text] [Related]
19. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease. Tomer G, Ceballos C, Concepcion E, Benkov KJ. Am J Gastroenterol; 2003 Nov 15; 98(11):2479-84. PubMed ID: 14638352 [Abstract] [Full Text] [Related]
20. Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation. Büning C, Genschel J, Bühner S, Krüger S, Kling K, Dignass A, Baier P, Bochow B, Ockenga J, Schmidt HH, Lochs H. Aliment Pharmacol Ther; 2004 May 15; 19(10):1073-8. PubMed ID: 15142196 [Abstract] [Full Text] [Related] Page: [Next] [New Search]